KPH · Class I · 21 CFR 876.5030

FDA Product Code KPH: Catheter, Rectal For Continent Ileostomy

1
Total
1
Cleared
17d
Avg days
1981
Since

FDA 510(k) Cleared Catheter, Rectal For Continent Ileostomy Devices (Product Code KPH)

1 devices
1–1 of 1
No devices found for this product code.

About Product Code KPH - Regulatory Context